Functional enhancer elements drive subclass-selective expression from mouse to primate neocortex
John K. Mich,
Lucas T. Graybuck,
Erik E. Hess,
Joseph T. Mahoney,
Jeremy A. Miller,
Nadiya V Shapovalova,
Refugio A. Martinez,
Kimberly A Smith,
Ryder P Gwinn,
Andrew L. Ko,
Jeffrey G Ojemann,
C. Dirk Keene,
Daniel L. Silbergeld,
Susan M. Sunkin,
Gregory D. Horwitz,
Ed S Lein,
Jonathan T Ting,
Boaz P. Levi
Posted 19 Feb 2019
bioRxiv DOI: 10.1101/555318
Posted 19 Feb 2019
Viral genetic tools to target specific brain cell types in humans and non-genetic model organisms will transform basic neuroscience and targeted gene therapy. Here we used comparative epigenetics to identify thousands of human neuronal subclass-specific putative enhancers to regulate viral tools, and 34% of these were conserved in mouse. We established an AAV platform to evaluate cellular specificity of functional enhancers by multiplexed fluorescent in situ hybridization (FISH) and single cell RNA sequencing. Initial testing in mouse neocortex yields a functional enhancer discovery success rate of over 30%. We identify enhancers with specificity for excitatory and inhibitory classes and subclasses including PVALB, LAMP5, and VIP/LAMP5 cells, some of which maintain specificity in vivo or ex vivo in monkey and human neocortex. Finally, functional enhancers can be proximal or distal to cellular marker genes, conserved or divergent across species, and could yield brain-wide specificity greater than the most selective marker genes. ### Competing Interest Statement JKM, LTG, EEH, HZ, BT, EL, JTT, and BPL are inventors on several U.S. provisional patent applications related to this work. All authors declare no other competing interests.
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